A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1445e214



Internal ID22757339
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:11732199..12080970hg38UCSC Ensembl
chr9:11732199..12080970hg19UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38348772
hg19348772
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3619631, esv3619630
SamplesHG03773, NA19222, HG01506, NA18747, NA18939, NA21141, HG01812, NA18610, HG00123, NA21091
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv1445e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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